ライフサイエンスコーパス: paraventricular nucleus

1 loops (by means of the nucleus reuniens and paraventricular nucleus).

2 releasing factor immunoreactive cells in the paraventricular nucleus.

3 e number of synapses has been doubled in the paraventricular nucleus.

4 ed c-fos mRNA expression in the hypothalamic paraventricular nucleus.

5 entromedial parvocellular subdivision of the paraventricular nucleus.

6 activity (indicating neuronal excitation) in paraventricular nucleus.

7 as found in the parvocellular portion of the paraventricular nucleus.

8 nd parvocellular neurons of the hypothalamic paraventricular nucleus.

9 elicited by stimulation of the hypothalamic paraventricular nucleus.

10 mpaired c-fos activation in the hypothalamic paraventricular nucleus.

11 -1Rs) in the vagus nerve, area postrema, and paraventricular nucleus.

12 within ACe and BnST, expression in thalamic paraventricular nucleus, a region involved in storing an

13 In the paraventricular nucleus, although temporal changes in ox

14 onents); behavior control column (descending paraventricular nucleus and associated arcuate nucleus;

15 neurons that express ENK in the hypothalamic paraventricular nucleus and central nucleus of the amygd

16 aled significantly less oxytocin mRNA in the paraventricular nucleus and increased oxytocin receptor

17 ated neuronal activation in the hypothalamic paraventricular nucleus and medial nucleus of the amygda

18 4Rs only in SIM1 neurons in the hypothalamic paraventricular nucleus and neurons in the amygdala was

19 , galanin, enkephalin, and dynorphin, in the paraventricular nucleus and orexin and melanin-concentra

20 s in Arc NPY projections areas (hypothalamic paraventricular nucleus and perifornical area) after Arc

21 ealed markedly enhanced galanin (GAL) in the paraventricular nucleus and reduced neuropeptide Y (NPY)

22 lar neuroendocrine cells of the hypothalamic paraventricular nucleus and supraoptic nucleus (SON) res

23 ut had normal activation in the hypothalamic paraventricular nucleus and the amygdalar central nucleu

24 er intake, was increased in the hypothalamic paraventricular nucleus and the subfornical organ.

25 amus was measured by c-fos expression in the paraventricular nucleus and the ventromedial preoptic ar

26 action, reduces melanocortin content in the paraventricular nucleus, and markedly increases suscepti

27 of the bed nucleus of the stria terminalis, paraventricular nucleus, and medial amygdala.

28 ary tract, periaqueductal gray, hypothalamic paraventricular nucleus, and medial preoptic area, sites

29 dalar nucleus (CAmy), anterior hypothalamus, paraventricular nucleus, and posterior lateral hypothala

30 and improving mitochondrial function in the paraventricular nucleus, and reveal multiple novel targe

31 twork (central amygdalar nucleus, descending paraventricular nucleus, and ventrolateral periaqueducta

32 ndant in the area postrema, arcuate nucleus, paraventricular nucleus, and ventromedial hypothalamus.

33 lateral hypothalamus, somatosensory cortex, paraventricular nucleus, and zona incerta; no regions we

34 in/proNKB fibers were also identified in the paraventricular nucleus, anterior hypothalamic area, med

35 The results showed increased c-Fos IR in the paraventricular nucleus, arcuate nucleus, central nucleu

36 easing hormone (TRH)-positive neurons in the paraventricular nucleus area of the hypothalamus and thu

37 n carotid bodies, striatum, and hypothalamic paraventricular nucleus, but not in the nucleus tractus

38 nucleus, ventromedial hypothalamic nucleus, paraventricular nucleus, dorsomedial hypothalamic nucleu

39 with RFRP-3 immunoreactivity enhanced in the paraventricular nucleus, dorsomedial nucleus, and Arc of

40 oinjection of muscimol into the hypothalamic paraventricular nucleus failed to reduce changes evoked

41 hanisms of chronic stress integration in the paraventricular nucleus, focusing on the role of glucoco

42 ngle-minded 1 neurons, we show dependence of paraventricular nucleus GLP-1 signaling in the coordinat

43 hypothalamic feeding nuclei/cell types, the paraventricular nucleus (GLP-1RKD(DeltaSim1cre)) and pro

44 The rat paraventricular nucleus has three major divisions: desce

45 n a modest increase in CRH expression in the paraventricular nucleus, hypoplastic adrenal glands and

46 le, the locus coeruleus, medial amygdala and paraventricular nucleus), implicating a prominent role o

47 oss of oxytocin (OT)-containing cells in the paraventricular nucleus in the hypothalamus (PVN; p<0.05

48 terminals, originating from the hypothalamic paraventricular nucleus, in the CA2 of mice.

49 Activation of the paraventricular nucleus is in-phase with the ipsilateral

50 brain barrier, but also in the hypothalamic paraventricular nucleus, located inside the blood brain

51 ion during the orgasms included hypothalamic paraventricular nucleus, medial amygdala, anterior cingu

52 with axonal projections to the hypothalamic paraventricular nucleus (MnPO-PVN) respond to osmotic, c

53 us (ARC; P < 0.05), and 50% in magnocellular paraventricular nucleus (mPVN; P < 0.05).

54 enetic stimulation of ARC TH axons inhibited paraventricular nucleus neurons by dopamine and GABA co-

55 of their postsynaptic targets (Arc POMC and paraventricular nucleus neurons), where ATP dramatically

56 at increased OT/c-fos colocalizations in the paraventricular nucleus of both sexes.

57 and increased mitochondrial function in the paraventricular nucleus of hypertensive rats by promotin

58 atory function in the supraoptic nucleus and paraventricular nucleus of hypertensive rats that contri

59 se system, and decreased inflammation in the paraventricular nucleus of hypertensive rats.

60 -2 fluorescence in perivascular cells of the paraventricular nucleus of hypothalamus, prostaglandin E

61 ied by reduced GLP-1 immunoreactivity in the paraventricular nucleus of hypothalamus, suggesting rele

62 Application of SP to the paraventricular nucleus of rats increases heart rate and

63 The paraventricular nucleus of thalamus (PVT), which project

64 stinct from that of Utx, specifically in the paraventricular nucleus of the hypothalamus (high Uty) a

65 ion between the circumventricular organs and paraventricular nucleus of the hypothalamus (PVH) and th

66 ve absent Crh mRNA and peptide mainly in the paraventricular nucleus of the hypothalamus (PVH) but pr

67 its were identified in subpopulations of the paraventricular nucleus of the hypothalamus (PVH) by dou

68 The paraventricular nucleus of the hypothalamus (PVH) consis

69 The paraventricular nucleus of the hypothalamus (PVH) contai

70 The paraventricular nucleus of the hypothalamus (PVH) coordi

71 The paraventricular nucleus of the hypothalamus (PVH) plays

72 e mediation of activational responses of the paraventricular nucleus of the hypothalamus (PVH) provok

73 ed mainly to the hypothalamus, including the paraventricular nucleus of the hypothalamus (PVH), later

74 altered POMC projections to the preautonomic paraventricular nucleus of the hypothalamus (PVH), pancr

75 utonomic nervous system, particularly in the paraventricular nucleus of the hypothalamus (PVH), play

76 ons provide a distinctive innervation of the paraventricular nucleus of the hypothalamus (PVH), with

77 tion factor necessary for development of the paraventricular nucleus of the hypothalamus (PVH).

78 f serotonin 2C receptors (5-HT(2C)Rs) in the paraventricular nucleus of the hypothalamus (PVH).

79 tream melanocortin-4 receptors (MC4R) in the paraventricular nucleus of the hypothalamus (PVH).

80 es in the anterior parvicellular part of the paraventricular nucleus of the hypothalamus (PVHap) and

81 xpression of IRS2 and TRPV1 receptors in the paraventricular nucleus of the hypothalamus (PVN) and do

82 reduced binding of both radioligands in the paraventricular nucleus of the hypothalamus (PVN) and me

83 tressors and are found within neurons of the paraventricular nucleus of the hypothalamus (PVN) and se

84 We tested the hypotheses that (1) the paraventricular nucleus of the hypothalamus (PVN) and th

85 e stress-related brain nuclei, including the paraventricular nucleus of the hypothalamus (PVN) and th

86 An increase in CRF mRNA in the paraventricular nucleus of the hypothalamus (PVN) and th

87 ation of firing activity of neurons from the paraventricular nucleus of the hypothalamus (PVN) by alp

88 d female rats, nanoinjection of NPY into the paraventricular nucleus of the hypothalamus (PVN) dose-d

89 ERalpha and produce vasopressin (AVP) in the paraventricular nucleus of the hypothalamus (PVN) in new

90 is critical for energy homeostasis, and the paraventricular nucleus of the hypothalamus (PVN) is a k

91 d the Cre/lox system to delete AT1a from the paraventricular nucleus of the hypothalamus (PVN) of mic

92 We found that neurons of the paraventricular nucleus of the hypothalamus (PVN) send d

93 e hypocretin neurons project directly to the paraventricular nucleus of the hypothalamus (PVN), and S

94 BST), central nucleus of the amygdala (CEA), paraventricular nucleus of the hypothalamus (PVN), and t

95 e profile of noradrenergic activity with the paraventricular nucleus of the hypothalamus (PVN), and t

96 tal cortex, striatum, nucleus accumbens, and paraventricular nucleus of the hypothalamus (PVN), in bo

97 and Fos immunoreactivity was measured in the paraventricular nucleus of the hypothalamus (PVN), the p

98 Bilateral nanoinjection of SHU9119 into the paraventricular nucleus of the hypothalamus (PVN), to bl

99 the hindbrain send robust projections to the paraventricular nucleus of the hypothalamus (PVN), which

100 mone (ACTH) secretagogue biosynthesis in the paraventricular nucleus of the hypothalamus (PVN).

101 rge part by noradrenergic (NA) inputs to the paraventricular nucleus of the hypothalamus (PVN).

102 the medial parvocellular subdivision of the paraventricular nucleus of the hypothalamus (PVN).

103 : the caudal ventrolateral medulla (CVLM) or paraventricular nucleus of the hypothalamus (PVN).

104 in G(s)alpha in brain regions outside of the paraventricular nucleus of the hypothalamus (PVN).

105 These neurons densely populate the paraventricular nucleus of the hypothalamus (PVN).

106 and oxytocin- (OC) containing neurons of the paraventricular nucleus of the hypothalamus (PVN).

107 mmunication in hypertension originating from paraventricular nucleus of the hypothalamus and presenti

108 n releasing factor-containing neurons of the paraventricular nucleus of the hypothalamus and primaril

109 ing was significantly greater in the AH, the paraventricular nucleus of the hypothalamus and the late

110 sympathoexcitatory brain centres such as the paraventricular nucleus of the hypothalamus and the rost

111 found that PACAP increased CRF levels in the paraventricular nucleus of the hypothalamus and, importa

112 c and anorexigenic neural projections to the paraventricular nucleus of the hypothalamus at PN 28.

113 hat knockdown of VP and OT production in the paraventricular nucleus of the hypothalamus exerts diver

114 tivate c-fos expression in the hind brain or paraventricular nucleus of the hypothalamus indicating t

115 in-releasing hormone (CRH) released from the paraventricular nucleus of the hypothalamus is a major r

116 -releasing factor type 1 receptor within the paraventricular nucleus of the hypothalamus is an import

117 ective activation of oxytocin neurons in the paraventricular nucleus of the hypothalamus stimulates i

118 g there make appositions onto neurons in the paraventricular nucleus of the hypothalamus that are als

119 tive axonal projections and terminals in the paraventricular nucleus of the hypothalamus, arcuate nuc

120 lateral bed nucleus of the stria terminalis, paraventricular nucleus of the hypothalamus, dorsal late

121 ular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalamus, IPe, arcuat

122 leasing hormone (Crh) gene expression in the paraventricular nucleus of the hypothalamus, the central

123 n type-1a receptor-containing neurons of the paraventricular nucleus of the hypothalamus, the goal be

124 olved in the development and function of the paraventricular nucleus of the hypothalamus.

125 parvocellular neurosecretory neurons of the paraventricular nucleus of the hypothalamus.

126 d nucleus of the stria terminalis (BNST) and paraventricular nucleus of the hypothalamus.

127 TS and reduction of GLP-1 innervation to the paraventricular nucleus of the hypothalamus.

128 ss responsiveness and transcriptomics of the paraventricular nucleus of the hypothalamus.

129 -releasing factor (CRF) immunodensity in the paraventricular nucleus of the hypothalamus.

130 e stria terminalis, and medial parvocellular paraventricular nucleus of the hypothalamus.

131 ormation and descending connections from the paraventricular nucleus of the hypothalamus.

132 in releasing hormone-positive neurons in the paraventricular nucleus of the hypothalamus.

133 is enriched in CRF-expressing neurons in the paraventricular nucleus of the hypothalamus.

134 with high levels of oxidative stress in the paraventricular nucleus of the hypothalamus.

135 effect that is dependent upon VDR within the paraventricular nucleus of the hypothalamus.

136 ssion in the brain that was localized to the paraventricular nucleus of the hypothalamus.

137 er, bed nucleus of the stria terminalis, and paraventricular nucleus of the hypothalamus.

138 mpanied by increased oxytocin release in the paraventricular nucleus of the hypothalamus.

139 ntified in 11 of 40 brain regions, including paraventricular nucleus of the hypothalamus; anterior an

140 precursor peptide, prepro-TRH (ppTRH) in the paraventricular nucleus of the rat hypothalamus and the

141 sted that OrxA transmission in the posterior paraventricular nucleus of the thalamus (pPVT) participa

142 We focus on the temporal recruitment of the paraventricular nucleus of the thalamus (PVT) for the re

143 Here we show a key role for the rat paraventricular nucleus of the thalamus (PVT), a nucleus

144 ian brain, one putative stress sensor is the paraventricular nucleus of the thalamus (PVT), an area t

145 The posterior paraventricular nucleus of the thalamus (THPVP) has been

146 entiates excitatory transmission between the paraventricular nucleus of the thalamus and D2-receptor-

147 Here we identify the paraventricular nucleus of the thalamus as a prominent i

148 Activity in the paraventricular nucleus of the thalamus to nucleus accum

149 ay- and cell-type-specific plasticity in the paraventricular nucleus of the thalamus to nucleus accum

150 The Gpr151-expressing neurons in the paraventricular nucleus of the thalamus was primarily co

151 ives dense DA innervation via the fr and the paraventricular nucleus of the thalamus, a stress sensit

152 of the stria terminalis (BNST), the anterior paraventricular nucleus of the thalamus, and the medial

153 observed in the cingulate cortex, posterior paraventricular nucleus of the thalamus, periaqueductal

154 lis in the telencephalon; habenular nucleus, paraventricular nucleus of the thalamus, preoptic area,

155 e midbrain periaqueductal gray (PAG) and the paraventricular nucleus of the thalamus, two brain areas

156 bed nuclei of the stria terminalis, and the paraventricular nucleus of the thalamus.

157 and some of which innervate both the PAG and paraventricular nucleus of the thalamus.

158 ation of GLP-1 into the arcuate, but not the paraventricular, nucleus of the hypothalamus reduced hep

159 ARC TH cells project to the hypothalamic paraventricular nucleus; optogenetic stimulation of ARC

160 Intra-paraventricular nucleus oxytocin injections reduced beha

161 Together, our data demonstrate that paraventricular nucleus oxytocin mediates the social buf

162 uropeptide Y (NPY) levels in the DMH and the paraventricular nucleus (P < 0.05).

163 TH release, in the parvocellular division of paraventricular nucleus (pcPVN), and (2) mFSS-induced ac

164 expression in the dorsomedial parvocellular paraventricular nucleus (pPVN) and increased anterior pi

165 g hormone (CRH) neurons in the parvocellular paraventricular nucleus (pPVN) play a key role in coordi

166 eurones in the parvocellular division of the paraventricular nucleus (pPVN) via noradrenergic (A2 cel

167 tion of BM-derived cells to the hypothalamic paraventricular nucleus, presumably via a mechanism of d

168 preoptic area (POA; homolog of the mammalian paraventricular nucleus), Purkinje cell layer of the cer

169 tidromically activated from the hypothalamic paraventricular nucleus (PVH) (latency: 10.3+/-1.3 ms, t

170 e Arc and its projection to the hypothalamic paraventricular nucleus (PVH) are both components of the

171 for glutamatergic input to the hypothalamic paraventricular nucleus (PVH) in stress-induced activati

172 ablished orexigenic peptide and hypothalamic paraventricular nucleus (PVH) is one major brain site th

173 ctivation of a pathway from the hypothalamic paraventricular nucleus (PVH) to the rostral ventrolater

174 ral brain regions including the hypothalamic paraventricular nucleus (PVH), the anteroventral periven

175 rticular attention to the innervation of the paraventricular nucleus (PVH), the dorsomedial nucleus (

176 and to the medial parvocellular part of the paraventricular nucleus (PVHmp).

177 ey rats with both a push-pull cannula in the paraventricular nucleus (PVN) and a catheter in the jugu

178 ors are highly expressed in the hypothalamic paraventricular nucleus (PVN) and arcuate nucleus (ARC).

179 ssure, and heart rate via projections to the paraventricular nucleus (PVN) and dorsomedial hypothalam

180 by parvocellular neurons of the hypothalamic paraventricular nucleus (PVN) and released into the port

181 ns in other hypothalamic regions such as the paraventricular nucleus (PVN) and rostral preoptic area

182 f E2 exposure, rats were sacrificed, and the paraventricular nucleus (PVN) and rostral ventrolateral

183 opressin (AVP) neurons from the hypothalamic paraventricular nucleus (PVN) and supraoptic nucleus (SO

184 CRF and oxytocin mRNA expression in the paraventricular nucleus (PVN) and supraoptic nucleus (SO

185 The paraventricular nucleus (PVN) and supraoptic nucleus (SO

186 The paraventricular nucleus (PVN) and supraoptic nucleus (SO

187 fspring stress regulating brain regions, the paraventricular nucleus (PVN) and the bed nucleus of str

188 These prominently included the hypothalamic paraventricular nucleus (PVN) and the nucleus of the sol

189 t the effects of NPS within the hypothalamic paraventricular nucleus (PVN) are mediated via actions o

190 tagonist) microinjected bilaterally into the paraventricular nucleus (PVN) attenuated the increase in

191 The paraventricular nucleus (PVN) contains spinally-projecti

192 sought to determine whether the hypothalamic paraventricular nucleus (PVN) contributes in a time-depe

193 The hypothalamic paraventricular nucleus (PVN) coordinates major neuroend

194 TP females had significantly lower values of paraventricular nucleus (PVN) corticotrophin releasing h

195 CRH mRNA expression in hypothalamic paraventricular nucleus (PVN) diminished after daily han

196 m laminae terminalis (OVLT) and hypothalamic paraventricular nucleus (PVN) each contribute significan

197 utyric acid (GABA)-projecting neurons in the paraventricular nucleus (PVN) have been shown to inhibit

198 in stimulates VP neurons in the hypothalamic paraventricular nucleus (PVN) in a nutritional state-dep

199 mmunolabeled cell nuclei in the hypothalamic paraventricular nucleus (PVN) in fasted as well as fed r

200 The paraventricular nucleus (PVN) in mammals is the main hyp

201 that NMU microinjected into the hypothalamic paraventricular nucleus (PVN) in rats increases the ener

202 osynthesis, in the arcuate nucleus (Arc) and paraventricular nucleus (PVN) in the hypothalamus.

203 ICER mRNA in the hypothalamic paraventricular nucleus (PVN) increased after 30 min and

204 Serotonergic agonists administered into the paraventricular nucleus (PVN) inhibit fat intake and ser

205 The hypothalamic paraventricular nucleus (PVN) integrates preautonomic an

206 The development of the hypothalamic paraventricular nucleus (PVN) involves several factors t

207 lenges such as dehydration, the hypothalamic paraventricular nucleus (PVN) is activated and drives SN

208 The hypothalamic paraventricular nucleus (PVN) is an important site modul

209 The hypothalamic paraventricular nucleus (PVN) is critically involved in

210 1 receptor (NMDA-NR1) expression within the paraventricular nucleus (PVN) is critically linked to th

211 (NMDA) receptor activity in the hypothalamic paraventricular nucleus (PVN) is crucial for the sympath

212 Increased glutamatergic input in the paraventricular nucleus (PVN) is important for high symp

213 NMDAR activity in the hypothalamic paraventricular nucleus (PVN) is increased and criticall

214 The hypothalamic paraventricular nucleus (PVN) is responsive to hypoxic s

215 hypothesis that neurons in the hypothalamic paraventricular nucleus (PVN) may be under both direct a

216 r GABA plays a key role in the modulation of paraventricular nucleus (PVN) neuronal excitability and

217 Despite the fact that paraventricular nucleus (PVN) neurones innervating the r

218 te mechanisms regulating the excitability of paraventricular nucleus (PVN) neurones that project dire

219 oxidase (NOX) in AVP-expressing hypothalamic paraventricular nucleus (PVN) neurons in "menopausal" fe

220 increased by angiotensin II (Ang II) within paraventricular nucleus (PVN) neurons of normotensive ra

221 e effects on stress-integrative hypothalamic paraventricular nucleus (PVN) neurons remains to be dete

222 c stressors via trans-synaptic influences on paraventricular nucleus (PVN) neurons.

223 flammatory cytokines activate neurons in the paraventricular nucleus (PVN) of hypothalamus, including

224 0delta mRNA was 1.5- to 2-fold higher in the paraventricular nucleus (PVN) of spontaneously hypertens

225 The paraventricular nucleus (PVN) of the hypothalamus contro

226 The paraventricular nucleus (PVN) of the hypothalamus is a k

227 -aspartate receptor (NMDAR) activity, in the paraventricular nucleus (PVN) of the hypothalamus is clo

228 d-aspartate receptor (NMDAR) activity in the paraventricular nucleus (PVN) of the hypothalamus is inv

229 Glutamatergic inputs in the paraventricular nucleus (PVN) of the hypothalamus mainta

230 rentiated neurons were transplanted into the paraventricular nucleus (PVN) of the hypothalamus of an

231 Preautonomic neurons in the paraventricular nucleus (PVN) of the hypothalamus play a

232 The paraventricular nucleus (PVN) of the hypothalamus plays

233 lls showing Fos immunoreactivity (ir) in the paraventricular nucleus (PVN) of the hypothalamus, the l

234 The hyperphagia derived from the paraventricular nucleus (PVN) of the hypothalamus, where

235 sed c-Fos immunoreactivity of neurons in the paraventricular nucleus (PVN) of the hypothalamus.

236 ttributable to global hypocellularity of the paraventricular nucleus (PVN) of the hypothalamus.

237 scription factor abundantly expressed in the paraventricular nucleus (PVN) of the hypothalamus.

238 1 and PC2 gene and protein expression in the paraventricular nucleus (PVN) of the hypothalamus.

239 rticotropin-releasing hormone (CRH) from the paraventricular nucleus (PVN) of the hypothalamus.

240 by microdialysis, either in the hypothalamic paraventricular nucleus (PVN) or in the ventromedial nuc

241 SB334867 microinjected into the hypothalamic paraventricular nucleus (PVN) or into the bed nucleus of

242 During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased.

243 amatergic synaptic input in the hypothalamic paraventricular nucleus (PVN) plays a critical role in r

244 thetic drive emanating from the hypothalamic paraventricular nucleus (PVN) plays a major role in the

245 The hypothalamic paraventricular nucleus (PVN) regulates numerous homeost

246 The paraventricular nucleus (PVN) regulates sympathetic outf

247 Hypothalamic projections from the paraventricular nucleus (PVN) release oxytocin (OT) to m

248 rolateral medulla (RVLM) from neurons in the paraventricular nucleus (PVN) that release arginine vaso

249 supports a contribution of the hypothalamic paraventricular nucleus (PVN) to sympathoexcitation and

250 Tmem18 expression in the murine hypothalamic paraventricular nucleus (PVN) was altered by changes in

251 At the end, the paraventricular nucleus (PVN) was analyzed by Real-time

252 In addition, activation of neurons in the paraventricular nucleus (PVN) was monitored by examining

253 actions of ANG II that are mediated via the paraventricular nucleus (PVN), an area that serves as a

254 or (CRF) mRNA expression in the hypothalamic paraventricular nucleus (PVN), and plasma cortisol and A

255 minalis (BNST), medial preoptic area (MPOA), paraventricular nucleus (PVN), anterior cortical (AcA),

256 Neuronal activity in the hypothalamic paraventricular nucleus (PVN), as well as sympathetic ou

257 a terminalis, central amygdala, hypothalamic paraventricular nucleus (PVN), Barrington's nucleus and

258 tic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN), dorsomedial nucleus (DM),

259 bited higher expression of 5HT2A mRNA in the paraventricular nucleus (PVN), higher expression of 5HT2

260 in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN), locus coeruleus (LC), ros

261 in the bed nucleus of the stria terminalis, paraventricular nucleus (PVN), posterior hypothalamus, p

262 Fos-ir activity was quantified in the paraventricular nucleus (PVN), subfornical organ (SFO),

263 Fos-like immunoreactive (IR) neurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON)

264 tor (CRF) mRNA and immunoreactive CRF in the paraventricular nucleus (PVN), the pituitary adrenocorti

265 The rostral region, containing the paraventricular nucleus (PVN), was defined by discrete l

266 ack CREB1 in SIM1-expressing neurons, of the paraventricular nucleus (PVN), which are known to be MC4

267 peptide levels in the anterior region of the paraventricular nucleus (PVN), with no change in the arc

268 um intake evoked an endogenous, hypothalamic paraventricular nucleus (PVN)-specific, decrease (sodium

269 on mediated in part through the hypothalamic paraventricular nucleus (PVN).

270 tor blockade in the ipsilateral hypothalamic paraventricular nucleus (PVN).

271 te several hypothalamic areas, including the paraventricular nucleus (PVN).

272 ERbeta immunoreactive cell numbers in ARH or paraventricular nucleus (PVN).

273 elicited by the stimulation of hypothalamic paraventricular nucleus (PVN).

274 ntact neurons projecting to the hypothalamic paraventricular nucleus (PVN).

275 l-regulated kinase (ERK) in the hypothalamic paraventricular nucleus (PVN).

276 or no direct projections to the hypothalamic paraventricular nucleus (PVN).

277 ventromedial (VMN) nucleus and parvocellular paraventricular nucleus (PVN).

278 and morphology of single neurons of the dog paraventricular nucleus (PVN).

279 -dependent dysregulation of the hypothalamic paraventricular nucleus (PVN).

280 rticotropin releasing hormone neurons in the paraventricular nucleus (PVN).

281 eptors (MC4R) in neurons of the hypothalamic paraventricular nucleus (PVN).

282 LHA (22%), zona incerta (ZI, 15%), CeA (5%), paraventricular nucleus (PVN, 13%), SLEA (66%), and MPA

283 RVLM-projecting neurons of the hypothalamic paraventricular nucleus (PVN-RVLM) contributes to an imb

284 the dorsomedial hypothalamus (including the paraventricular nucleus [PVN]) but not in the pituitary

285 were counted in the posterior portion of the paraventricular nucleus (PVNp), supraoptic nucleus (SON)

286 havior control column (ingestive: descending paraventricular nucleus; reproductive: lateral medial pr

287 Transcriptomic analysis of the paraventricular nucleus revealed widespread changes in e

288 autonomic brain regions (i.e., hypothalamic paraventricular nucleus, rostral ventrolateral medulla a

289 damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insuli

290 unexpectedly, emanates from the hypothalamic paraventricular nucleus, specifically from subsets of ne

291 m hypothalamic neuroendocrine neurons in the paraventricular nucleus stimulates neighboring (~100 mum

292 entricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprachiasmatic nucleus, and ve

293 were high in, for example, piriform cortex, paraventricular nucleus, supraoptic nucleus, arcuate nuc

294 c area, the bed nuclei stria terminalis, the paraventricular nucleus thalamus, and the anterior hypot

295 ng hormone (CRH) neurons in the hypothalamic paraventricular nucleus that govern neuroendocrine stres

296 ns, including the arcuate nucleus (ARC), the paraventricular nucleus, the medial preoptic area, the l

297 ns from oxytocin neurons in the hypothalamic paraventricular nucleus to midbrain DA regions.

298 nate extract reduces oxidative stress in the paraventricular nucleus to relieve hypertension.

299 rticotrophin releasing factor neurons in the paraventricular nucleus, which when activated result in

300 llular and magnocellular subdivisions of the paraventricular nucleus, with greater increases ipsilate